Seeing haemoglobin SC: Challenging the misperceptions-Reference-Cited by-同舟云学术

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Seeing haemoglobin SC: Challenging the misperceptions

Published:2024-06-23 Issue:2 Volume:205 Page:404-405
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Segbefia Catherine¹^ORCID,Luchtman‐Jones Lori²³^ORCID

Affiliation:

1. Department of Child Health University of Ghana Medical School Accra Ghana

2. Division of Hematology Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

3. Department of Pediatrics University of Cincinnati College of Medicine Cincinnati Ohio USA

Abstract

Historically understudied and regarded as a mild type of sickle cell disease, HbSC can be associated with significant, progressive complications. Prospective studies are urgently needed to address treatment gaps for HbSC disease.Commentary on: Nelson et al. The clinical spectrum of HbSC sickle cell disease‐not a benign condition. Br J Haematol 2024;205:653‐663.

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.19580

Reference8 articles.

1. Knowledge insufficient: the management of haemoglobin SC disease

2. Implementing newborn screening for sickle cell disease in Korle Bu Teaching Hospital, Accra: Results and lessons learned

3. The paradox of hemoglobin SC disease

4. The clinical spectrum of HbSC sickle cell disease‐not a benign condition

5. Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death

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